Related Experiment Video
Updated: May 11, 2025

High-speed Video Microscopy Analysis for First-line Diagnosis of Primary Ciliary Dyskinesia
Published on: January 19, 2022
Caroli Syndrome: Challenges in Early Diagnosis for Infants
Olfa Asbik1, Amal Hamami1, Abdeladim Babakhouya1
1Department of Pediatrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Mohammed I University of Oujda, Oujda, MAR.
Abstract:
Caroli syndrome is an uncommon disorder characterized by congenital, segmental dilation of the intrahepatic bile ducts, often widespread and accompanied by liver fibrosis, progressing to juvenile portal hypertension. Although present at birth, this congenital anomaly is often undetected until adulthood. The diagnosis is usually delayed due to its clinical latency. In this case, a one-year-and-eight-month-old infant with abdominal distension and hepatosplenomegaly underwent imaging, which revealed segmental dilation of the intrahepatic bile ducts. Early detection allowed for timely management, reducing the risk of severe complications. Early diagnosis of Caroli syndrome in infants is rare but crucial to preventing severe complications such as recurrent cholangitis, liver fibrosis, and portal hypertension. Physicians should maintain a high index of suspicion for Caroli syndrome in cases of persistent abdominal distension, as early recognition can facilitate appropriate imaging, timely intervention, and improved patient outcomes.
Related Concept Videos
Imaging Studies for Cardiovascular System III: X-Ray
Definition and Purpose
An X-ray, or radiograph, is a non-invasive method that uses ionizing radiation to take images of internal structures. It is mainly used in cardiac imaging to examine the heart, lungs, and major blood vessels, aiming to identify abnormalities in the heart's size, shape, and position, such as heart failure, congenital defects, and vascular...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...

